Post-Surgical Mesh - ANVISA Registration 82765310012

Access comprehensive regulatory information for Post-Surgical Mesh in Brazil's medical device market through Pure Global AI's free database. This Risk Class I medical device is registered under ANVISA number 82765310012 and manufactured by BOA FORMA CONFECÇÕES LTDA. The registration is held by BOA FORMA CONFECÇÕES LTDA with validity until currently active (VIGENTE).

This page provides complete technical specifications for this device, regulatory compliance details, 5 similar products found using AI-powered semantic search, 5 companies making the same product including Plie Confecções Ltda, BOA FORMA CONFECÇÕES LTDA, and 5 recent registrations in the same technical category. Pure Global AI offers free access to over 100,000+ Brazilian medical device registrations, helping global MedTech companies navigate ANVISA regulations, identify competitors, and discover partnership opportunities efficiently.